Canonical Allele Identifier: CA2082754657

Gene: BRCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32328035_32328039delinsCACCT , CM000675.2:g.32328035_32328039delinsCACCT	GRCh38
NC_000013.10:g.32902172_32902176delinsCACCT , CM000675.1:g.32902172_32902176delinsCACCT	GRCh37
NC_000013.9:g.31800172_31800176delinsCACCT	NCBI36
NG_012772.3:g.17556_17560delinsCACCT , LRG_293:g.17556_17560delinsCACCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.632-1408_632-1404delinsCACCT	ENSP00000434898.2:n.632-1408_632-1404delinsCACCT
ENST00000528762.2:c.632-1408_632-1404delinsCACCT	ENSP00000433168.2:n.632-1408_632-1404delinsCACCT
ENST00000530893.7:c.263-1408_263-1404delinsCACCT	ENSP00000499438.2:n.263-1408_263-1404delinsCACCT
ENST00000665585.2:c.632-1408_632-1404delinsCACCT	ENSP00000499570.2:n.632-1408_632-1404delinsCACCT
ENST00000666593.2:c.632-1408_632-1404delinsCACCT	ENSP00000499256.2:n.632-1408_632-1404delinsCACCT
ENST00000700202.2:c.632-1408_632-1404delinsCACCT	ENSP00000514856.2:n.632-1408_632-1404delinsCACCT
ENST00000700201.1:c.*411-1408_*411-1404delinsCACCT	ENSP00000514855.1:n.*411-1408_*411-1404delinsCACCT
ENST00000380152.8:c.632-1408_632-1404delinsCACCT MANE Select	ENSP00000369497.3:n.632-1408_632-1404delinsCACCT
ENST00000544455.6:c.632-1408_632-1404delinsCACCT	ENSP00000439902.1:n.632-1408_632-1404delinsCACCT
ENST00000614259.2:c.632-1408_632-1404delinsCACCT	ENSP00000506251.1:n.632-1408_632-1404delinsCACCT
ENST00000680887.1:c.632-1408_632-1404delinsCACCT	ENSP00000505508.1:n.632-1408_632-1404delinsCACCT
ENST00000380152.7:c.632-1408_632-1404delinsCACCT	ENSP00000369497.3:n.632-1408_632-1404delinsCACCT
ENST00000530893.6:n.830-1408_830-1404delinsCACCT
ENST00000544455.5:c.632-1408_632-1404delinsCACCT	ENSP00000439902.1:n.632-1408_632-1404delinsCACCT
ENST00000614259.1:n.632-1408_632-1404delinsCACCT
NM_000059.3:c.632-1408_632-1404delinsCACCT , LRG_293t1:c.632-1408_632-1404delinsCACCT	NP_000050.2:n.632-1408_632-1404delinsCACCT
XM_011535203.1:c.632-1408_632-1404delinsCACCT	XP_011533505.1:n.632-1408_632-1404delinsCACCT
XM_011535204.1:c.632-1408_632-1404delinsCACCT	XP_011533506.1:n.632-1408_632-1404delinsCACCT
XM_011535205.1:c.632-1408_632-1404delinsCACCT	XP_011533507.1:n.632-1408_632-1404delinsCACCT
NM_000059.4:c.632-1408_632-1404delinsCACCT MANE Select	NP_000050.3:n.632-1408_632-1404delinsCACCT